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Filters: Keyword is Genotype  [Clear All Filters]
Pedneault M, Labbe A, Roy-Gagnon M-H, Low NC, Dugas E, Engert JC, O'Loughlin J.  2014.  The association between CHRN genetic variants and dizziness at first inhalation of cigarette smoke.. Addict Behav. 39(1):316-20.
Silveira PPelufo, Portella AKrumel, Kennedy JL, Gaudreau H, Davis C, Steiner M, Soares CN, Matthews SG, Sokolowski MB, Dubé L et al..  2014.  Association between the seven-repeat allele of the dopamine-4 receptor gene (DRD4) and spontaneous food intake in pre-school children.. Appetite. 73:15-22.
Choudhry Z, Sengupta S, Thakur G, Page V, Schmitz N, Grizenko N, Joober R.  2014.  Catechol-o-methyltransferase gene and executive function in children with ADHD.. J Atten Disord. 18(3):202-11.
Teh ALing, Pan H, Chen L, Ong M-L, Dogra S, Wong J, MacIsaac JL, Mah SM, McEwen LM, Saw S-M et al..  2014.  The effect of genotype and in utero environment on interindividual variation in neonate DNA methylomes.. Genome Res. 24(7):1064-74.
O'Donnell K, Glover V, Holbrook JD, O'Connor TG.  2014.  Maternal prenatal anxiety and child brain-derived neurotrophic factor (BDNF) genotype: effects on internalizing symptoms from 4 to 15 years of age.. Dev Psychopathol. 26(4 Pt 2):1255-66.
Zhang R, Li X, Ramaswami G, Smith KS, Turecki G, Montgomery SB, Li JBilly.  2014.  Quantifying RNA allelic ratios by microfluidic multiplex PCR and sequencing.. Nat Methods. 11(1):51-4.
Blumenthal I, Ragavendran A, Erdin S, Klei L, Sugathan A, Guide JR, Manavalan P, Zhou JQ, Wheeler VC, Levin JZ et al..  2014.  Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families.. Am J Hum Genet. 94(6):870-83.